RECALL RECORD — CLASS IIIRecall closedF-1304-2013/FDA enforcement

Ferrous Sulfate Tablets 325 mg, 100 Count Bottles, Nutritional Supplement

What you need to know

Class III
  • What happened

    The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameMagno Humphries INC
Recalling firmMagno Humphries INCTigard, OR, United States
UPC / barcodes
0 43292 56306 0
Lot / date codes
  • Product code -L6430-100-01(L is designate label, 6430 is the firm's internal product code, 100 is for 100 count and 01 stands for Optimum label, and 0 is the firm's version number. All of these products have the same label code, however
  • they have different lot numbers. Lot Numbers: 343617, 343718, 343739, 343753, 343814, 343888, and 343959. Expiration dates 11/15, 12/15, 12/15, 12/15, 12/15, 1/16 and 1/16 respectively (expiration dates are month and year) The lot number and expiration date is stamped on the bottom of the bottles.
Distribution area
Nationwide

Distributed to only one consignee with several locations nationwide.

United States

Quantity affected40369 bottles
Recall initiationFDA report date: April 17, 2013
FDA recall numberF-1304-2013

Beyond the headline

The recall, in context

Magno Humphries INC initiated this supplements recall on March 18, 2013. The FDA enforcement report states: The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic. The FDA report lists distribution as: Distributed to only one consignee with several locations nationwide.

The FDA enforcement report describes the reason as: The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.

Ferrous Sulfate Tablets 325 mg, 100 Count Bottles, Nutritional Supplement was made or distributed by Magno Humphries INC in Tigard, OR, United States. This page reflects FDA report F-1304-2013, dated April 17, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Plastic contamination

Possible health effects

Plastic fragments can pose a choking risk or cause irritation or injury to the mouth and digestive tract.

Higher-risk groups

Young children and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product and do not taste or chew it to check for fragments.
  2. 2Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Ferrous Sulfate Tablets 325 mg, 100 Count Bottles, Nutritional Supplement recall?

Magno Humphries INC recalled Ferrous Sulfate Tablets 325 mg, 100 Count Bottles, Nutritional Supplement in an FDA Class III enforcement action reported as F-1304-2013. The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop eating or using the product and do not taste or chew it to check for fragments. Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Magno Humphries INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1304-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.